Results 311 to 320 of about 89,084 (326)
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Medium chain acyl-coenzyme A dehydrogenase deficiency.
New Jersey medicine : the journal of the Medical Society of New Jersey, 1992Medium chain acyl-coenzyme A dehydrogenase deficiency (MCADD) was the first metabolic disorder found to be associated with sudden infant death syndrome. This review covers recent advances in the biochemical and molecular understanding of MCADD.
M J, Bennett, D E, Hale
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15 Acyl Coenzyme A: Cholesterol O-Acyltransferase
1983Publisher Summary This chapter focuses on Acyl coenzyme A: cholesterol O -acyltransferase (ACAT), which utilizes long-chain fatty acyl coenzyme A and cholesterol as substrates to catalyze the formation of cholesterol esters. This enzyme is responsible for the cellular synthesis of cholesterol esters in various cell types. The presence of cholesterol-
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LC-MS/MS-based analysis of coenzyme A and short-chain acyl-coenzyme A thioesters
Analytical and Bioanalytical Chemistry, 2015S. Neubauer +5 more
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Regulation of pyruvate carboxylase by coenzyme A and acyl coenzyme A thio esters
Biochemistry, 1968T C, Cooper, C R, Benedict
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Possible Reaction Pathway for Acylation of Coenzyme A
Journal of Pharmaceutical Sciences, 1971openaire +2 more sources
[Acyl-coenzyme A: cholesterol acyltransferase (ACAT)].
Nihon rinsho. Japanese journal of clinical medicine, 2005Akira, Miyazaki, Takuya, Watanabe
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